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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307670Generated: November 1, 2026

3-Hydroxybenzaldehyde → 3-(Allyloxy)benzaldehyde

https://huagongshe.com/reaction/2307670

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantAllyl bromideHCID 7841—
ReactantCesium carbonateHCID 10796—
SolventDiethyl EtherHCID 3283—
SolventDimethylacetamideHCID 31374—
Product3-(Allyloxy)benzaldehydeHCID 271661289.6%

Reaction Steps

3-Hydroxybenzaldehyde (1.00 g, 8.19 mmol) and allyl bromide (0.780 mL, 9.01 mmol) in N,N-dimethylacetamide (35 mL) was treated with Cs2CO3 (4.01 g, 12.3 mmol) and allowed to stir at room temperature for 12 hours. The reaction mixture was diluted with diethyl ether (150 mL), washed with 1N HCl, saturated NaHCO3, brine, dried (MgSO4), filtered and the filtrate concentrated. The residue was purified by flash chromatography (silica gel, using 7% ethyl acetate/hexanes as eluent) to provide the title compound as a clear oil (1.19 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06831193B2
Source datasetuspto-grants-2004_12
ORD IDord-5dd646a2b3a142b2bce2412fd8f27925
Source noteuspto-grants-2004_12